Podcast
Questions and Answers
Which T cell type secretes IFN-γ and IL-2 to activate macrophages and cytotoxic T cells?
Which T cell type secretes IFN-γ and IL-2 to activate macrophages and cytotoxic T cells?
- Th2
- Treg
- Th1 (correct)
- Th17
What is the function of Th2 cells in the immune response?
What is the function of Th2 cells in the immune response?
- Prevent autoimmunity
- Induce neutrophilic inflammation
- Activate macrophages and cytotoxic T cells
- Activate eosinophils and increase IgE production (correct)
Where does positive selection of T cells occur?
Where does positive selection of T cells occur?
- Thymic medulla
- Peripheral blood
- Thymic cortex (correct)
- Bone marrow
Which T cell type is involved in inducing neutrophilic inflammation?
Which T cell type is involved in inducing neutrophilic inflammation?
Deficiency in which molecule leads to autoimmune polyendocrine syndrome-1?
Deficiency in which molecule leads to autoimmune polyendocrine syndrome-1?
What is the main role of Th1 cells in the immune response?
What is the main role of Th1 cells in the immune response?
Which T cell type is involved in preventing autoimmunity and maintaining tolerance?
Which T cell type is involved in preventing autoimmunity and maintaining tolerance?
Where do T cells expressing TCRs with high affinity for self antigens undergo apoptosis or become regulatory T cells?
Where do T cells expressing TCRs with high affinity for self antigens undergo apoptosis or become regulatory T cells?
What is the main function of Th2 cells in the immune response?
What is the main function of Th2 cells in the immune response?
Which molecule plays a crucial role in maintaining tolerance and preventing autoimmunity?
Which molecule plays a crucial role in maintaining tolerance and preventing autoimmunity?
Flashcards
Robertsonian Translocation
Robertsonian Translocation
A type of chromosomal abnormality where the long arms of two acrocentric chromosomes fuse at the centromere, resulting in the loss of short arms.
Balanced Translocations
Balanced Translocations
Translocations where the total amount of genetic material remains unchanged, typically without noticeable phenotypic effects.
Unbalanced Translocations
Unbalanced Translocations
Translocations where there is missing or extra genetic material, leading to various conditions and developmental issues.
Cri-du-Chat Syndrome
Cri-du-Chat Syndrome
Signup and view all the flashcards
Hexokinase
Hexokinase
Signup and view all the flashcards
Glucokinase
Glucokinase
Signup and view all the flashcards
Glycolysis
Glycolysis
Signup and view all the flashcards
Alanine
Alanine
Signup and view all the flashcards
McArdle Disease
McArdle Disease
Signup and view all the flashcards
Lysosomal Storage Diseases
Lysosomal Storage Diseases
Signup and view all the flashcards
Study Notes
- Translocation is a common type of chromosomal abnormality, specifically Robertsonian translocation.
- Occurs when long arms of two acrocentric chromosomes fuse at the centromere, resulting in loss of short arms.
- Balanced translocations usually do not cause any noticeable phenotype, as genetic material remains unchanged.
- Unbalanced translocations, which involve missing or extra genes, can lead to various conditions and developmental issues.
- Cri-du-chat syndrome is an example of an unbalanced translocation resulting from the deletion of a part of chromosome 5's short arm (5p−).
- Characterized by microcephaly, moderate to severe intellectual disability, high-pitched crying, epicanthal folds, and cardiac abnormalities, such as a ventricular septal defect (VSD).
- Williams syndrome is another example of an unbalanced translocation, caused by the deletion of a part of the long arm of chromosome 7 (7q−).
- Features include distinctive "elfin" facies, intellectual disability, well-developed verbal skills, hypercalcemia, extreme friendliness towards strangers, and absorbed cardiovascular problems, such as supravalvular aortic stenosis and renal artery stenosis.
- Essential fatty acids, polyunsaturated fatty acids, are crucial nutrients that cannot be synthesized in the body.
- Hexokinase and glucokinase are enzymes responsible for converting glucose into glucose-6-phosphate, with different locations, affinities, and induced effects.
- Hexokinase is located in most tissues except the liver and pancreatic β cells.
- Glucokinase is mainly found in the liver and pancreatic β cells.
- Glycolysis is a metabolic process converting glucose into pyruvate, yielding ATP and NADH.
- Regulated by glucose-6-phosphate, which can inhibit or activate hexokinase and glucokinase.
- Amino acid metabolism and transport play a significant role in the body.
- Alanine is a critical player in the transfer of ammonia from muscle to the liver through the Cahill cycle.
- McArdle disease (type V) affects muscle glycogen metabolism, leading to painful muscle cramps, myoglobinuria, and arrhythmias during strenuous exercise.
- Lysosomal storage diseases result from deficiencies in lysosomal enzymes and the accumulation of abnormal metabolic products.
- Various diseases, such as Tay-Sachs, Niemann-Pick, and some forms of Gaucher disease, are examples of lysosomal storage diseases.
- Immunology is the study of the immune system, including cellular components and their functions.
- T cells are essential components of the immune system, differentiating from T cell precursors in the bone marrow and thymus.
- Thymus is crucial for the selection, maturation, and survival of T cells.
- Double-positive T cells (CD4+/CD8+) expressing TCRs capable of binding selfMHC on cortical epithelial cells survive, whereas those with high affinity for self antigens undergo apoptosis or become regulatory T cells.
- Macrophages and T cells interact through various cytokines and chemokines, leading to the activation and killing of microbes.
Studying That Suits You
Use AI to generate personalized quizzes and flashcards to suit your learning preferences.
